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51679-41-5

51679-41-5

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51679-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51679-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,7 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51679-41:
(7*5)+(6*1)+(5*6)+(4*7)+(3*9)+(2*4)+(1*1)=135
135 % 10 = 5
So 51679-41-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H10F3NO3/c15-14(16,17)21-10-7-5-9(6-8-10)18-12-4-2-1-3-11(12)13(19)20/h1-8,18H,(H,19,20)

51679-41-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[4-(trifluoromethoxy)anilino]benzoic acid

1.2 Other means of identification

Product number -
Other names Benzoic acid,2-((4-(trifluoromethoxy)phenyl)amino)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:51679-41-5 SDS

51679-41-5Downstream Products

51679-41-5Relevant articles and documents

Redox-neutral decarboxylative photocyclization of anthranilic acids

Huang, Huawen,Deng, Kun,Deng, Guo-Jun

supporting information, p. 8243 - 8247 (2020/12/29)

A mild metal-, catalyst-, and oxidant-free photoredox neutral system has been found to efficiently enable intramolecular decarboxylative cyclization of anthranilic acids. This facile protocol provides an alternative method for the synthesis of carbazoles. Mechanistic studies reveal a key photoinduced 6π-electrocyclization process and formic acid was released as the sole byproduct.

Convenient access to substituted acridines by a Buchwald-Hartwig amination

Csuk, René,Barthel, Alexander,Raschke, Christian

, p. 5737 - 5750 (2007/10/03)

A convenient, high yield procedure for the synthesis of anthranilic acids carrying a variety of different substituents as well as their straightforward transformation into the corresponding 9-chloroacridines could be established by using modified Buchwald-Hartwig amination conditions.

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